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ISCA1P1 iron-sulfur cluster assembly 1 pseudogene 1 [ Homo sapiens (human) ]

Gene ID: 389293, updated on 10-Dec-2019

Summary

Official Symbol
ISCA1P1provided by HGNC
Official Full Name
iron-sulfur cluster assembly 1 pseudogene 1provided by HGNC
Primary source
HGNC:HGNC:33263
Gene type
pseudo
RefSeq status
INFERRED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
ISCA1L

Genomic context

See ISCA1P1 in Genome Data Viewer
Location:
5q12.1
Annotation release Status Assembly Chr Location
109.20191205 current GRCh38.p13 (GCF_000001405.39) 5 NC_000005.10 (62775369..62777343, complement)
105 previous assembly GRCh37.p13 (GCF_000001405.25) 5 NC_000005.9 (62071203..62073171, complement)

Chromosome 5 - NC_000005.10Genomic Context describing neighboring genes Neighboring gene importin 11 Neighboring gene IPO11-LRRC70 readthrough Neighboring gene ribosomal protein L35a pseudogene 14 Neighboring gene leucine rich repeat containing 70 Neighboring gene dedicator of cytokinesis 9 pseudogene Neighboring gene uncharacterized LOC107986418

Genomic regions, transcripts, and products

Phenotypes

NHGRI GWAS Catalog

Description
A genome-wide association study (GWAS) for bronchopulmonary dysplasia.
NHGRI GWA Catalog
A genome-wide association study of serum uric acid in African Americans.
NHGRI GWA Catalog
Genome-wide contribution of genotype by environment interaction to variation of diabetes-related traits.
NHGRI GWA Catalog

NCBI Reference Sequences (RefSeq)

RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

  1. NG_021247.2 

    Range
    101..2075
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

RefSeqs of Annotated Genomes: Homo sapiens Updated Annotation Release 109.

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p13 Primary Assembly

Genomic

  1. NC_000005.10 Reference GRCh38.p13 Primary Assembly

    Range
    62775369..62777343 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Suppressed Reference Sequence(s)

The following Reference Sequences have been suppressed. Explain

  1. NM_001080540.1: Suppressed sequence

    Description
    NM_001080540.1: This RefSeq was permanently suppressed because it is now thought that this gene is a pseudogene.
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